A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3689n106



Internal ID19021798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:147186864..147187077hg38UCSC Ensembl
chr7:146883956..146884169hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1112161, nsv1135252
SamplesKWS2
Known GenesCNTNAP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3689n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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